rs1801002(G;T)

Carrier of a recessive deafness mutation

Is a	genotype
of	rs1801002
Gene	GJB2
Chromosome	13
Position	20,189,547
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	3	Carrier of a recessive deafness mutation
(GT;GT)	0	common in clinvar
(I;I)	0

see GJB2 and deafness